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Bacterial biofilm functionalization through Bap amyloid engineering
Biofilm engineering has emerged as a controllable way to fabricate living structures with programmable functionalities. The amyloidogenic proteins comprising the biofilms can be engineered to create self-assembling extracellular functionalized surfaces. In this regard, facultative amyloids, which pl...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9339546/ https://www.ncbi.nlm.nih.gov/pubmed/35909185 http://dx.doi.org/10.1038/s41522-022-00324-w |
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author | Matilla-Cuenca, Leticia Taglialegna, Agustina Gil, Carmen Toledo-Arana, Alejandro Lasa, Iñigo Valle, Jaione |
author_facet | Matilla-Cuenca, Leticia Taglialegna, Agustina Gil, Carmen Toledo-Arana, Alejandro Lasa, Iñigo Valle, Jaione |
author_sort | Matilla-Cuenca, Leticia |
collection | PubMed |
description | Biofilm engineering has emerged as a controllable way to fabricate living structures with programmable functionalities. The amyloidogenic proteins comprising the biofilms can be engineered to create self-assembling extracellular functionalized surfaces. In this regard, facultative amyloids, which play a dual role in biofilm formation by acting as adhesins in their native conformation and as matrix scaffolds when they polymerize into amyloid-like fibrillar structures, are interesting candidates. Here, we report the use of the facultative amyloid-like Bap protein of Staphylococcus aureus as a tool to decorate the extracellular biofilm matrix or the bacterial cell surface with a battery of functional domains or proteins. We demonstrate that the localization of the functional tags can be change by simply modulating the pH of the medium. Using Bap features, we build a tool for trapping and covalent immobilizing molecules at bacterial cell surface or at the biofilm matrix based on the SpyTag/SpyCatcher system. Finally, we show that the cell wall of several Gram-positive bacteria could be functionalized through the external addition of the recombinant engineered Bap-amyloid domain. Overall, this work shows a simple and modulable system for biofilm functionalization based on the facultative protein Bap. |
format | Online Article Text |
id | pubmed-9339546 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-93395462022-08-02 Bacterial biofilm functionalization through Bap amyloid engineering Matilla-Cuenca, Leticia Taglialegna, Agustina Gil, Carmen Toledo-Arana, Alejandro Lasa, Iñigo Valle, Jaione NPJ Biofilms Microbiomes Article Biofilm engineering has emerged as a controllable way to fabricate living structures with programmable functionalities. The amyloidogenic proteins comprising the biofilms can be engineered to create self-assembling extracellular functionalized surfaces. In this regard, facultative amyloids, which play a dual role in biofilm formation by acting as adhesins in their native conformation and as matrix scaffolds when they polymerize into amyloid-like fibrillar structures, are interesting candidates. Here, we report the use of the facultative amyloid-like Bap protein of Staphylococcus aureus as a tool to decorate the extracellular biofilm matrix or the bacterial cell surface with a battery of functional domains or proteins. We demonstrate that the localization of the functional tags can be change by simply modulating the pH of the medium. Using Bap features, we build a tool for trapping and covalent immobilizing molecules at bacterial cell surface or at the biofilm matrix based on the SpyTag/SpyCatcher system. Finally, we show that the cell wall of several Gram-positive bacteria could be functionalized through the external addition of the recombinant engineered Bap-amyloid domain. Overall, this work shows a simple and modulable system for biofilm functionalization based on the facultative protein Bap. Nature Publishing Group UK 2022-08-01 /pmc/articles/PMC9339546/ /pubmed/35909185 http://dx.doi.org/10.1038/s41522-022-00324-w Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Matilla-Cuenca, Leticia Taglialegna, Agustina Gil, Carmen Toledo-Arana, Alejandro Lasa, Iñigo Valle, Jaione Bacterial biofilm functionalization through Bap amyloid engineering |
title | Bacterial biofilm functionalization through Bap amyloid engineering |
title_full | Bacterial biofilm functionalization through Bap amyloid engineering |
title_fullStr | Bacterial biofilm functionalization through Bap amyloid engineering |
title_full_unstemmed | Bacterial biofilm functionalization through Bap amyloid engineering |
title_short | Bacterial biofilm functionalization through Bap amyloid engineering |
title_sort | bacterial biofilm functionalization through bap amyloid engineering |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9339546/ https://www.ncbi.nlm.nih.gov/pubmed/35909185 http://dx.doi.org/10.1038/s41522-022-00324-w |
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